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723286-79-1

723286-79-1 Structure

723286-79-1 Structure
IdentificationBack Directory
[Name]

5,6-DIHYDRO-8H-[1,2,4]TRIAZOLO[4,3-A]PYRAZINE-7-CARBOXYLIC ACID TERT-BUTYL ESTER
[CAS]

723286-79-1
[Synonyms]

7-N-Boc-5,6-dihydro-8H-[1,2,4]triazolo[4,3-a]pyrazine
7-Boc-5,6,7,8-tetrahydro-1,2,4-triazolo[4,3-a]pyrazine
tert-Butyl 5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazine-7(8H)
5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazine-7(8H)-carboxylate
tert-butyl 5H,6H,7H,8H-[1,2,4]triazolo[4,3-a]pyrazine-7-carboxylate
TERT-BUTYL 5,6-DIHYDRO-[1,2,4]TRIAZOLO[4,3-A]PYRAZINE-7(8H)-CARBOXYLATE
tert-Butyl 5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazine-7(8H)-carboxylate ,99%
5,6-DIHYDRO-8H-[1,2,4]TRIAZOLO[4,3-A]PYRAZINE-7-CARBOXYLIC ACID TERT-BUTYL ESTER
tert-butyl 5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazine-7(8H)-carboxylate hydrochloride
1,2,4-Triazolo[4,3-a]pyrazine-7(8H)-carboxylic acid, 5,6-dihydro-, 1,1-dimethylethyl ester
[Molecular Formula]

C10H16N4O2
[MDL Number]

MFCD10574958
[MOL File]

723286-79-1.mol
[Molecular Weight]

224.26
Chemical PropertiesBack Directory
[Boiling point ]

378.4±52.0 °C(Predicted)
[density ]

1.28±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,2-8°C
[pka]

2.87±0.20(Predicted)
[Appearance]

White to off-white Solid
Safety DataBack Directory
[HS Code ]

29349990
Hazard InformationBack Directory
[Chemical Properties]

Off-white solid
[Synthesis]

8-CHLORO-[1,2,4]TRIAZOLO[4,3-A]PYRAZINE

68774-77-6

Di-tert-butyl dicarbonate

24424-99-5

5,6-DIHYDRO-8H-[1,2,4]TRIAZOLO[4,3-A]PYRAZINE-7-CARBOXYLIC ACID TERT-BUTYL ESTER

723286-79-1

8-Chloro-[1,2,4]triazolo[4,3-A]pyrazine (8.10 g) obtained in Step 2 was mixed with platinum (IV) oxide and 10% palladium/carbon (2 g, 50% aqueous content) in methanol (8 mL) and placed under a hydrogen atmosphere (50 psi, Parr unit) and stirred for 34 hours. Upon completion of the reaction, the reaction mixture was filtered through a Hyflo Super Cel and the filtrate was concentrated to give an oil. The oil was dissolved in dichloromethane (200 mL) and N,N-diisopropylethylamine (10 mL) and di-tert-butyl dicarbonate (11.4 g) were added sequentially and the reaction was stirred for 3 hours at room temperature. At the end of the reaction, saturated aqueous sodium bicarbonate solution was added and extracted with chloroform three times. The organic layers were combined, dried with anhydrous sodium sulfate and concentrated. The resulting crude product was purified by silica gel column chromatography to afford 7-Boc-5,6,7,8-tetrahydro-1,2,4-triazolo[4,3-a]pyrazine (2.55 g, 22% yield).

[References]

[1] Patent: JP5851663, 2016, B1. Location in patent: Paragraph 0302
Spectrum DetailBack Directory
[Spectrum Detail]

5,6-DIHYDRO-8H-[1,2,4]TRIAZOLO[4,3-A]PYRAZINE-7-CARBOXYLIC ACID TERT-BUTYL ESTER(723286-79-1)1HNMR
5,6-DIHYDRO-8H-[1,2,4]TRIAZOLO[4,3-A]PYRAZINE-7-CARBOXYLIC ACID TERT-BUTYL ESTER(723286-79-1)1HNMR
5,6-DIHYDRO-8H-[1,2,4]TRIAZOLO[4,3-A]PYRAZINE-7-CARBOXYLIC ACID TERT-BUTYL ESTER(723286-79-1)13CNMR
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